ARHGAP11B Rho GTPase activating protein 11B

Information
Symbol
ARHGAP11B
Type
protein-coding
Description
Rho GTPase activating protein 11B
Entrez Gene ID
89839
Genome
hg19
Position
chr15:30,918,169-30,941,732
Genome
hg38
Position
chr15:30,625,966-30,649,529
MIM
616310 OMIM
HGNC
HGNC:15782 HGNC
Ensembl
ENSG00000285077 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 4
not provided 5 0
Uncertain significance 0 30
Ranking
ClinVar
0
0
0
34
0
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Variant name Gene AA change CDS Japanese
frequency		 TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence		 Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM B'-T
SYNONYM FAM7B1
SYNONYM GAP (1-8)
MIM 616310 OMIM
HGNC HGNC:15782 HGNC
Ensembl ENSG00000285077 Ensembl
AllianceGenome HGNC:15782
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000693711.1 hg38 chr15 30,625,966 30,649,529 23,564
ENST00000697964.2 hg38 chr15 30,626,128 30,638,810 12,683
ENST00000428041.4 hg38 chr15 30,625,966 30,649,529 23,564
ENST00000428041.4 hg19 chr15 30,918,169 30,941,732 23,564
ENST00000693711.1 hg19 chr15 30,918,169 30,941,732 23,564
ENST00000697964.2 hg19 chr15 30,918,331 30,931,013 12,683
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